Were hiring: Clinical Data Specialist Clinical Data Management (Mexico)
Location: Mexico (candidates must be currently based in Mexico)
Do you enjoy turning complex lab data into clean reliable clinical insights Join our Clinical Data Management team as a Clinical Data Specialist and play a key role in ensuring highquality local laboratory data that supports the success of global clinical trials. Youll collaborate with crossfunctional teams and external partners (labs/CROs) helping drive accuracy compliance and operational excellence from study startup through database lock.
What youll do
- Support local laboratory data activities for clinical studies (inhouse and outsourced) ensuring timely and highquality deliverables
- Review study protocols and local lab requirements to identify required analytes
- Maintain and support a Global Analyte Library aligned with internal laboratory standards
- Partner with Clinical Operations Biometrics Medical Monitoring and Regulatory teams to align lab data with study timelines and milestones
- Proactively identify risks and issues related to lab data collection transfer and quality and support mitigation plans
- Configure laboratory locations and analyte parameters in systems such as Veeva Vault Local Lab Module
- Champion continuous improvement initiatives including process optimization automation and adoption of new technologies
What youll bring
- 2 years of experience in Clinical Data Management and/or the drug development process
- Strong knowledge of local laboratory data management within clinical trials
- Familiarity with ICH/GCP and regulatory standards applicable to clinical data
- Ability to manage multiple studies or priorities in a fastpaced global environment
- Bachelors degree in life sciences healthrelated or technologyrelated field (or equivalent experience)
Why this role Youll have direct impact on data integrity and trial success work in a collaborative global environment and further develop your expertise in a highdemand area of clinical research.
Important: This role is based in Mexico and we can only consider candidates currently located in Mexico.
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
Were hiring: Clinical Data Specialist Clinical Data Management (Mexico) Location: Mexico (candidates must be currently based in Mexico)Do you enjoy turning complex lab data into clean reliable clinical insights Join our Clinical Data Management team as a Clinical Data Specialist and play a key rol...
Were hiring: Clinical Data Specialist Clinical Data Management (Mexico)
Location: Mexico (candidates must be currently based in Mexico)
Do you enjoy turning complex lab data into clean reliable clinical insights Join our Clinical Data Management team as a Clinical Data Specialist and play a key role in ensuring highquality local laboratory data that supports the success of global clinical trials. Youll collaborate with crossfunctional teams and external partners (labs/CROs) helping drive accuracy compliance and operational excellence from study startup through database lock.
What youll do
- Support local laboratory data activities for clinical studies (inhouse and outsourced) ensuring timely and highquality deliverables
- Review study protocols and local lab requirements to identify required analytes
- Maintain and support a Global Analyte Library aligned with internal laboratory standards
- Partner with Clinical Operations Biometrics Medical Monitoring and Regulatory teams to align lab data with study timelines and milestones
- Proactively identify risks and issues related to lab data collection transfer and quality and support mitigation plans
- Configure laboratory locations and analyte parameters in systems such as Veeva Vault Local Lab Module
- Champion continuous improvement initiatives including process optimization automation and adoption of new technologies
What youll bring
- 2 years of experience in Clinical Data Management and/or the drug development process
- Strong knowledge of local laboratory data management within clinical trials
- Familiarity with ICH/GCP and regulatory standards applicable to clinical data
- Ability to manage multiple studies or priorities in a fastpaced global environment
- Bachelors degree in life sciences healthrelated or technologyrelated field (or equivalent experience)
Why this role Youll have direct impact on data integrity and trial success work in a collaborative global environment and further develop your expertise in a highdemand area of clinical research.
Important: This role is based in Mexico and we can only consider candidates currently located in Mexico.
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
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